Canonical Allele Identifier: CA519277900
Gene: EMD HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153608108G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379748G>A , CM000685.2:g.154379748G>A GRCh38
NC_000023.10:g.153608108G>A , CM000685.1:g.153608108G>A GRCh37
NC_000023.9:g.153261302G>A NCBI36
NG_008677.1:g.10313G>A , LRG_745:g.10313G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.141G>A ENSP00000507245.1:p.Arg47=
ENST00000682478.1:n.117G>A
ENST00000683576.1:n.117G>A
ENST00000683627.1:c.141G>A ENSP00000507533.1:p.Arg47=
ENST00000684082.1:c.141G>A ENSP00000508266.1:p.Arg47=
ENST00000684633.1:n.113G>A
ENST00000684678.1:c.137G>A ENSP00000507059.1:p.Gly46Asp
ENST00000369842.9:c.141G>A MANE Select ENSP00000358857.4:p.Arg47=
ENST00000369835.3:c.82+182G>A ENSP00000358850.3:n.82+182G>A
ENST00000369842.8:c.141G>A ENSP00000358857.4:p.Arg47=
ENST00000428228.5:c.*46G>A ENSP00000401081.1:n.*46G>A
ENST00000468294.5:n.101G>A
ENST00000485261.1:n.163+182G>A
ENST00000486738.5:n.285G>A
ENST00000492448.1:n.124G>A
ENST00000494443.5:n.198G>A
NM_000117.2:c.141G>A , LRG_745t1:c.141G>A NP_000108.1:p.Arg47=
XM_024452349.1:c.-68G>A XP_024308117.1:n.-68G>A
NM_000117.3:c.141G>A MANE Select NP_000108.1:p.Arg47=